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ManaMed

FDA UDI

Class I (US FDA UDI)

by Manamed Llc

Identity

Trade Name
ManaMed FDA UDI
Generic Name
Lumbar spine orthosis FDA UDI
Device Name
The Tailback 50 is a universal spinal orthosis designed with our patent pending chord compression system with center hub compression technology. It is designed to provide a rigid, comfortable, and quick fitting solution for every patient. Ice pack included. Easy application, universal size Removable ice pack Lightweight, latex free breathable material Single pulley system FDA UDI
Model / Reference
Tailback 50 FDA UDI
Description
The Tailback 50 is a universal spinal orthosis designed with our patent pending chord compression system with center hub compression technology. It is designed to provide a rigid, comfortable, and quick fitting solution for every patient. Ice pack included. Easy application, universal size Removable ice pack Lightweight, latex free breathable material Single pulley system FDA UDI

Identifiers

Catalog Number
TB050 FDA UDI
Primary DI / UDI-DI
00810113681900 FDA UDI
FDA Product Code
IQE FDA UDI
GMDN Term
Lumbar spine orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3490 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

ManaMed by Manamed Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Manamed Llc

Sources (1)

  • FDA UDI f543666a-1753-4f31-ae57-183d98e05d26 35 fields · synced May 31, 2026